Acoustic neuroma

听神经瘤
  • 文章类型: Journal Article
    背景:前庭神经鞘瘤(VS)的治疗包括在保守的“等待和扫描”(WAS)方法之间进行选择,立体定向放射外科(SRS)或开放显微外科切除术。目前,关于中小型VS的优化管理方法没有共识。这项研究旨在比较接受WAS和SRS初始治疗的中小型VS患者与听力相关的结果。
    方法:使用PubMed/MEDLINE对现有文献进行了系统综述,Embase,和Cochrane在2023年12月8日。使用随机效应模型进行Meta分析,以计算平均差(MD)和相对风险(RR)。进行了留一法分析。通过非随机研究干预中的偏倚风险(ROBINS-I)和Cochrane偏倚风险评估工具(RoB-2)评估偏倚风险。最终,使用GRADE评估对证据的确定性进行评估.主要结果是有用的听力,和纯音平均(PTA)。次要结果是Penn听神经瘤生活质量量表(PANQOL)总分。
    结果:有9项研究符合纳入条件,共1,275名患者。其中,674(52.86%)接受了WAS,601例患者(47.14%)接受SRS。随访时间为2至8年。荟萃分析表明,WAS对有用的听力有更好的结果(0.47;95%CI:0.32-0.68;p<0.001),以及术后功能测量,包括PTA评分(MD13.48;95%CI3.83-23.13;p<0.01),和PANQOL总分(MD3.83;95%CI0.42-7.25;p=0.03)。证据的总体确定性范围从“非常低”到“中等”。
    结论:与SRS相比,用WAS治疗中小型VS增加了保留可用听力和优化PANQOL术后总评分的可能性。然而,在现有研究中观察到的文献有限和方法学缺陷概述了对更高质量研究的需求.
    BACKGROUND: The management of vestibular schwannomas (VS) encompasses a choice between conservative \"wait-and-scan\" (WAS) approach, stereotactic radiosurgery (SRS) or open microsurgical resection. Currently, there is no consensus on the optimal management approach for small to medium sized VS. This study aims to compared outcomes related to hearing in patients with small and medium sized VS who underwent initial treatment with WAS versus SRS.
    METHODS: A systematic review of the available literature was conducted using PubMed/MEDLINE, Embase, and Cochrane up December 08, 2023. Meta-analysis was performed using a random-effect model to calculate mean difference (MD) and relative risk (RR). A leave-one-out analysis was conducted. The risk of bias was assessed via the Risk of Bias in Non-randomized Studies-Interventions (ROBINS-I) and Cochrane Risk of Bias assessment tool (RoB-2). Ultimately, the certainty of evidence was evaluated using the GRADE assessment. The primary outcomes were serviceable hearing, and pure-tone average (PTA). The secondary outcome was the Penn Acoustic Neuroma Quality of Life Scale (PANQOL) total score.
    RESULTS: Nine studies were eligible for inclusion, comprising a total of 1,275 patients. Among these, 674 (52.86%) underwent WAS, while 601 patients (47.14%) received SRS. Follow-up duration ranged from two to eight years. The meta-analysis indicated that WAS had a better outcome for serviceable hearing (0.47; 95% CI: 0.32 - 0.68; p < 0.001), as well as for postoperative functional measures including PTA score (MD 13.48; 95% CI 3.83 - 23.13; p < 0.01), and PANQOL total score (MD 3.83; 95% CI 0.42 - 7.25; p = 0.03). The overall certainty of evidence ranged from \"very low\" to \"moderate\".
    CONCLUSIONS: Treating small to medium sized VS with WAS increases the likelihood of preserving serviceable hearing and optimized PANQOL overall postoperative score compared to SRS. Nevertheless, the limited availability of literature and the methodological weakness observed in existing studies outline the need for higher-quality studies.
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  • 文章类型: Journal Article
    背景:本综述的目的是评估人类观察研究提供的证据的质量和强度,以证明暴露于射频电磁场(RF-EMF)与大多数研究的肿瘤疾病的风险之间存在因果关系。
    方法:合格标准:我们纳入了与三种类型的RF-EMF暴露有关的肿瘤形成风险的队列和病例对照研究:近场,头部局部化,无线电话使用暴露(SR-A);远场,整个身体,固定站点发射器(SR-B)的环境暴露;在工作场所使用手持式收发器或RF发射设备(SR-C)的近/远场职业暴露。虽然对肿瘤类型没有限制,在当前的论文中,我们专注于对选定的“关键”中枢神经系统肿瘤(脑,脑膜,脑垂体,听神经)和唾液腺肿瘤(SR-A);脑肿瘤和白血病(SR-B,SR-C)。我们专注于与特定暴露源(即E-O对)相关的特定肿瘤的调查,注意,一篇文章可能涉及多个E-O对。
    方法:通过Medline的文献检索确定了符合条件的研究,Embase,和EMF门户。偏倚风险(RoB)评估:我们使用了健康评估和翻译办公室(OHAT)RoB工具的定制版本来评估每个研究的内部有效性。在总结RoB步骤中,根据研究的总体偏见潜力将研究分为三个层次(低,中等和高)。
    结果:我们使用随机效应限制最大似然(REML)模型(二分和分类暴露变量的总体和亚组荟萃分析)综合了研究结果,和加权混合效应模型(终生暴露强度的剂量-反应荟萃分析)。证据评估:使用建议分级评估对证据的信心,评估,开发和评估(等级)方法。
    结果:我们纳入了63篇病因学文章,1994年至2022年出版,来自22个国家的参与者,报告119个不同的E-O对。手机的RF-EMF暴露(曾经或定期使用与没有或不定期使用)与胶质瘤的风险增加无关[相对风险(mRR)的meta估计=1.01,95%CI=0.89-1.13),脑膜瘤(mRR=0.92,95%CI=0.82-1.02),听神经瘤(mRR=1.03,95%CI=0.85-1.24),垂体肿瘤(mRR=0.81,95%CI=0.61-1.06),唾液腺肿瘤(mRR=0.91,95%CI=0.78-1.06),或儿科(儿童,青少年和年轻人)脑肿瘤(mRR=1.06,95%CI=0.74-1.51),具有不同程度的跨研究异质性(I2=0%-62%)。对于研究最多的肿瘤(神经胶质瘤,脑膜瘤,和听神经瘤)随着手机开始(TSS)使用时间的增加,累计通话时间(CCT),或累计通话次数(CNC)。无绳电话使用与脑膜瘤[mRR=1.04,95%CI=0.74-1.46;I2=74%](mRR=0.91,95%CI=0.70-1.18;I2=59%),或听神经瘤(mRR=1.16;95%CI=0.83-1.61;I2=63%)。固定站点发射器(广播天线或基站)的暴露与儿童白血病或小儿脑瘤风险无关,与模拟的射频暴露水平无关。职业性射频暴露后胶质瘤风险没有显著增加(从未与从未),并且在建模的累积暴露水平的增加类别之间没有检测到差异。
    结论:在胶质瘤的敏感性分析中,脑膜瘤,和与手机使用相关的听神经瘤风险(曾经使用过,TSS,CCT,和CNC)提出的结果是稳健的,不受研究聚集变化的影响。在与手机使用相关的神经胶质瘤风险的留一荟萃分析中,我们确定了一项有影响力的研究。在排除本研究后进行的后续荟萃分析中,我们观察到mRR的大幅降低和研究之间的异质性,对于对比剂,从未使用(常规)(mRR=0.96,95%CI=0.87-1.07,I2=47%),在增加TSS类别的分析中(“<5年”:mRR=0.97,95%CI=0.83-1.14,I2=41%;“5-9年”:mRR=0.96,95%CI=0.83-1.11,I2=34%;“10年”:mRR=0.97,95%CI=0.87-1.08,I2=10%)。RoB中优先领域的研究差异有限(选择/减员,暴露和结果信息),研究数量均匀地分为低和中等偏倚风险(49%的一级和51%的二级),没有被归类为高偏倚风险的研究(第3层)。偏差对研究结果(数量和方向)的影响难以预测,而RoB工具本来就无法解释竞争偏见的影响。然而,敏感性荟萃分析按偏倚层分层,表明,在我们的主要荟萃分析中观察到的异质性,在TSS上层的神经胶质瘤和听神经瘤的研究中(I2=77%和76%),由摘要RoB-tier解释。在一级研究亚组中,长期(10年以上)用户的mRRs(95%CI;I2)是胶质瘤的0.95(0.85-1.05;5.5%),听神经瘤为1.00(0.78-1.29;35%)。时间趋势模拟研究,根据外部有效性的三角剖分方法评估为补充证据,这表明在一些病例对照研究中观察到的增加的风险与在几个国家和长期观察到的神经胶质瘤/脑癌的实际发病率不相容。这些模拟研究中的三个一致报道,在10年以上的诱导期,RR估计值>1.5肯定是不可信的,并可用于设置“信誉基准”。在TSS上层类胶质瘤风险的敏感性荟萃分析中,不包括5项报告不合理效应大小的研究,我们观察到mRR[mRR为0.95(95%CI=0.86-1.05)]的显著降低,以及不同研究的异质性程度(I2=3.6%)。
    结论:与已发布的方案一致,我们的最终结论是针对每个暴露-结果组合单独制定的,主要基于最高可信度的证据,考虑到从剂量学研究中推断的按暴露水平对RF源的排名,以及与时间趋势模拟研究结果的外部一致性(仅限于与手机使用有关的神经胶质瘤)。对于从手机使用到头部的近场RF-EMF暴露,有适度的确定性证据表明它可能不会增加神经胶质瘤的风险,脑膜瘤,听神经瘤,垂体肿瘤,成人的唾液腺肿瘤,或小儿脑肿瘤。对于从无绳电话使用到头部的近场RF-EMF暴露,有低确定性的证据表明它可能不会增加神经胶质瘤的风险,脑膜瘤或听神经瘤。对于来自固定站点发射器(广播天线或基站)的全身远场RF-EMF暴露,有中度确定性证据表明它可能不会增加儿童白血病的风险,而低确定性证据表明它可能不会增加儿童脑肿瘤的风险.没有适合纳入研究的研究来自固定站点发射器和成人关键肿瘤的RF-EMF暴露。对于职业性RF-EMF暴露,有低确定性证据表明它可能不会增加脑癌/神经胶质瘤的风险,但没有纳入白血病(SR-C的第二个关键结局)的研究.应谨慎解释儿科脑肿瘤与固定部位发射器环境射频暴露相关的证据评级。由于研究数量少。类似的解释性警告适用于神经胶质瘤/脑癌与职业性射频暴露之间关系的证据评级。由于少数纳入研究的暴露来源和指标存在差异。
    该项目由世界卫生组织(WHO)委托和部分资助。共同供资由新西兰卫生部提供;IstitutoSuperiorediSanità作为世卫组织辐射与健康合作中心;ARPANSA作为世卫组织辐射防护合作中心。
    背景:PROSPEROCRD42021236798。公布的协议:[(Lagorio等人,2021)DOIhttps://doi.org/10.1016/j。envint.2021.106828]。
    BACKGROUND: The objective of this review was to assess the quality and strength of the evidence provided by human observational studies for a causal association between exposure to radiofrequency electromagnetic fields (RF-EMF) and risk of the most investigated neoplastic diseases.
    METHODS: Eligibility criteria: We included cohort and case-control studies of neoplasia risks in relation to three types of exposure to RF-EMF: near-field, head-localized, exposure from wireless phone use (SR-A); far-field, whole body, environmental exposure from fixed-site transmitters (SR-B); near/far-field occupational exposures from use of hand-held transceivers or RF-emitting equipment in the workplace (SR-C). While no restrictions on tumour type were applied, in the current paper we focus on incidence-based studies of selected \"critical\" neoplasms of the central nervous system (brain, meninges, pituitary gland, acoustic nerve) and salivary gland tumours (SR-A); brain tumours and leukaemias (SR-B, SR-C). We focussed on investigations of specific neoplasms in relation to specific exposure sources (i.e. E-O pairs), noting that a single article may address multiple E-O pairs.
    METHODS: Eligible studies were identified by literature searches through Medline, Embase, and EMF-Portal. Risk-of-bias (RoB) assessment: We used a tailored version of the Office of Health Assessment and Translation (OHAT) RoB tool to evaluate each study\'s internal validity. At the summary RoB step, studies were classified into three tiers according to their overall potential for bias (low, moderate and high).
    RESULTS: We synthesized the study results using random effects restricted maximum likelihood (REML) models (overall and subgroup meta-analyses of dichotomous and categorical exposure variables), and weighted mixed effects models (dose-response meta-analyses of lifetime exposure intensity). Evidence assessment: Confidence in evidence was assessed using the Grading of Recommendations, Assessment, Development and Evaluations (GRADE) approach.
    RESULTS: We included 63 aetiological articles, published between 1994 and 2022, with participants from 22 countries, reporting on 119 different E-O pairs. RF-EMF exposure from mobile phones (ever or regular use vs no or non-regular use) was not associated with an increased risk of glioma [meta-estimate of the relative risk (mRR) = 1.01, 95 % CI = 0.89-1.13), meningioma (mRR = 0.92, 95 % CI = 0.82-1.02), acoustic neuroma (mRR = 1.03, 95 % CI = 0.85-1.24), pituitary tumours (mRR = 0.81, 95 % CI = 0.61-1.06), salivary gland tumours (mRR = 0.91, 95 % CI = 0.78-1.06), or paediatric (children, adolescents and young adults) brain tumours (mRR = 1.06, 95 % CI = 0.74-1.51), with variable degree of across-study heterogeneity (I2 = 0 %-62 %). There was no observable increase in mRRs for the most investigated neoplasms (glioma, meningioma, and acoustic neuroma) with increasing time since start (TSS) use of mobile phones, cumulative call time (CCT), or cumulative number of calls (CNC). Cordless phone use was not significantly associated with risks of glioma [mRR = 1.04, 95 % CI = 0.74-1.46; I2 = 74 %) meningioma, (mRR = 0.91, 95 % CI = 0.70-1.18; I2 = 59 %), or acoustic neuroma (mRR = 1.16; 95 % CI = 0.83-1.61; I2 = 63 %). Exposure from fixed-site transmitters (broadcasting antennas or base stations) was not associated with childhood leukaemia or paediatric brain tumour risks, independently of the level of the modelled RF exposure. Glioma risk was not significantly increased following occupational RF exposure (ever vs never), and no differences were detected between increasing categories of modelled cumulative exposure levels.
    CONCLUSIONS: In the sensitivity analyses of glioma, meningioma, and acoustic neuroma risks in relation to mobile phone use (ever use, TSS, CCT, and CNC) the presented results were robust and not affected by changes in study aggregation. In a leave-one-out meta-analyses of glioma risk in relation to mobile phone use we identified one influential study. In subsequent meta-analyses performed after excluding this study, we observed a substantial reduction in the mRR and the heterogeneity between studies, for both the contrast Ever vs Never (regular) use (mRR = 0.96, 95 % CI = 0.87-1.07, I2 = 47 %), and in the analysis by increasing categories of TSS (\"<5 years\": mRR = 0.97, 95 % CI = 0.83-1.14, I2 = 41 %; \"5-9 years \": mRR = 0.96, 95 % CI = 0.83-1.11, I2 = 34 %; \"10+ years\": mRR = 0.97, 95 % CI = 0.87-1.08, I2 = 10 %). There was limited variation across studies in RoB for the priority domains (selection/attrition, exposure and outcome information), with the number of studies evenly classified as at low and moderate risk of bias (49 % tier-1 and 51 % tier-2), and no studies classified as at high risk of bias (tier-3). The impact of the biases on the study results (amount and direction) proved difficult to predict, and the RoB tool was inherently unable to account for the effect of competing biases. However, the sensitivity meta-analyses stratified on bias-tier, showed that the heterogeneity observed in our main meta-analyses across studies of glioma and acoustic neuroma in the upper TSS stratum (I2 = 77 % and 76 %), was explained by the summary RoB-tier. In the tier-1 study subgroup, the mRRs (95 % CI; I2) in long-term (10+ years) users were 0.95 (0.85-1.05; 5.5 %) for glioma, and 1.00 (0.78-1.29; 35 %) for acoustic neuroma. The time-trend simulation studies, evaluated as complementary evidence in line with a triangulation approach for external validity, were consistent in showing that the increased risks observed in some case-control studies were incompatible with the actual incidence rates of glioma/brain cancer observed in several countries and over long periods. Three of these simulation studies consistently reported that RR estimates > 1.5 with a 10+ years induction period were definitely implausible, and could be used to set a \"credibility benchmark\". In the sensitivity meta-analyses of glioma risk in the upper category of TSS excluding five studies reporting implausible effect sizes, we observed strong reductions in both the mRR [mRR of 0.95 (95 % CI = 0.86-1.05)], and the degree of heterogeneity across studies (I2 = 3.6 %).
    CONCLUSIONS: Consistently with the published protocol, our final conclusions were formulated separately for each exposure-outcome combination, and primarily based on the line of evidence with the highest confidence, taking into account the ranking of RF sources by exposure level as inferred from dosimetric studies, and the external coherence with findings from time-trend simulation studies (limited to glioma in relation to mobile phone use). For near field RF-EMF exposure to the head from mobile phone use, there was moderate certainty evidence that it likely does not increase the risk of glioma, meningioma, acoustic neuroma, pituitary tumours, and salivary gland tumours in adults, or of paediatric brain tumours. For near field RF-EMF exposure to the head from cordless phone use, there was low certainty evidence that it may not increase the risk of glioma, meningioma or acoustic neuroma. For whole-body far-field RF-EMF exposure from fixed-site transmitters (broadcasting antennas or base stations), there was moderate certainty evidence that it likely does not increase childhood leukaemia risk and low certainty evidence that it may not increase the risk of paediatric brain tumours. There were no studies eligible for inclusion investigating RF-EMF exposure from fixed-site transmitters and critical tumours in adults. For occupational RF-EMF exposure, there was low certainty evidence that it may not increase the risk of brain cancer/glioma, but there were no included studies of leukemias (the second critical outcome in SR-C). The evidence rating regarding paediatric brain tumours in relation to environmental RF exposure from fixed-site transmitters should be interpreted with caution, due to the small number of studies. Similar interpretative cautions apply to the evidence rating of the relation between glioma/brain cancer and occupational RF exposure, due to differences in exposure sources and metrics across the few included studies.
    UNASSIGNED: This project was commissioned and partially funded by the World Health Organization (WHO). Co-financing was provided by the New Zealand Ministry of Health; the Istituto Superiore di Sanità in its capacity as a WHO Collaborating Centre for Radiation and Health; and ARPANSA as a WHO Collaborating Centre for Radiation Protection.
    BACKGROUND: PROSPERO CRD42021236798. Published protocol: [(Lagorio et al., 2021) DOI https://doi.org/10.1016/j.envint.2021.106828].
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  • 文章类型: Case Reports
    钙通道阻滞剂(CCB)通常用于多种疾病的治疗,包括高血压,心律失常,血管痉挛症.尼莫地平,二氢吡啶CCB,已证明可在前庭神经鞘瘤切除手术后保留听力。由于它的广泛使用,CCB过量是常见的。该病例报告介绍了一名56岁女性患有终末期肝功能障碍的CCB毒性独特病例。前庭神经鞘瘤手术后接受单剂量预防性尼莫地平后,患者出现血管舒张性休克。本报告的主要目的是强调在围手术期接受尼莫地平治疗的晚期肝病患者存在CCB毒性的独特风险。
    Calcium channel blockers (CCBs) are commonly used in the management of multiple diseases, including hypertension, arrhythmia, and vasospastic disorder. Nimodipine, a dihydropyridine CCB, has demonstrated utility in preserving hearing following vestibular schwannoma resection surgery. Due to its widespread use, CCB overdose is common. This case report presents a unique case of CCB toxicity in a 56-year-old female with end-stage liver dysfunction. The patient developed vasodilatory shock after receiving a single dose of prophylactic nimodipine following vestibular schwannoma surgery. The primary objective of this report is to highlight the unique risk for CCB toxicity that exists for patients with advanced liver disease who receive nimodipine in the perioperative setting.
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  • 文章类型: Journal Article
    目的:确定听神经瘤患者显微外科手术后味觉障碍的发生率。
    方法:根据PRISMA指南进行系统评价和荟萃分析。彻底搜索PubMed/Medline,Cochrane系统评价数据库,和Epistemonikos进行了直到2024年5月16日发表的研究,报告了听神经瘤显微外科手术干预后的术后味觉障碍率。通过非随机研究方法学指数(MINORS)工具评估纳入研究的方法学质量。使用MedCalc(v.20.215)软件,随机效应模型用于比例荟萃分析.
    结果:八项研究,涵盖2,402名患者(平均年龄=49.06岁;48.54%的女性人口),包括在分析中。听神经瘤显微手术治疗后味觉障碍的总体合并率为23.7%(95%CI:9.266-42.359,p<0.0001)。当通过手术方法分层时,乙状窦后入路术后味觉障碍发生率为18.8%(95%CI:2.821-44.461,p<0.0001)。任何纳入的研究均未报告其他主要显微外科手术方法(颞下和经唇鼻法)分层的术后味觉障碍数据。
    结论:我们的系统评价和荟萃分析计算出近25%的对照率,并认为术后味觉障碍是听神经瘤显微外科治疗后常见的并发症。这些结果突出了术前咨询的重要性以及在听神经瘤的显微外科干预期间将对鼓索神经的损害可能性降至最低的策略的制定。
    OBJECTIVE: To determine the collated rate of postoperative dysgeusia after microsurgical intervention in acoustic neuroma patients.
    METHODS: The systematic review with meta-analysis was undertaken following PRISMA guidelines. A thorough search of PubMed/Medline, the Cochrane Database of Systematic Reviews, and Epistemonikos was undertaken for studies published up until May 16, 2024 reporting postoperative taste disturbance rates after microsurgical intervention for acoustic neuroma. The methodological quality of the included studies was assessed via the Methodological Index for Non-Randomized research (MINORS) tool. Using MedCalc (v. 20.215) software, the random-effects model was developed for proportional meta-analysis.
    RESULTS: Eight studies, encompassing 2,402 patients (mean age = 49.06 years; 48.54% female population), were included in the analysis. The overall pooled rate of postoperative dysgeusia following microsurgical management of acoustic neuroma was 23.7% (95% CI: 9.266-42.359, p < 0.0001). When stratified by surgical approach, the rate of postoperative dysgeusia for the retrosigmoid approach was 18.8% (95% CI: 2.821-44.461, p < 0.0001). Postoperative dysgeusia data stratified for other major microsurgical approaches (subtemporal and translabirynthine approaches) was not reported by any of the included studies.
    CONCLUSIONS: Our systematic review and meta-analysis calculated a collated rate of almost 25% and recognized postoperative dysgeusia as a common complication following microsurgical management of acoustic neuromas. These results highlight the significance of preoperative counselling and the development of strategies that minimize the likelihood of harm to the chorda tympani nerve during microsurgical intervention for acoustic neuroma.
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  • 文章类型: Journal Article
    OBJECTIVE: Acoustic neuroma (AN) is a benign tumor that usually affects a patient\'s hearing and balance function. For the screening and diagnosis of AN, the traditional approach mainly relies on audiological examination and magnetic resonance imaging (MRI), often ignoring the importance of vestibular function assessment in the affected area. As an emerging method of vestibular function detection, video head impulse test (vHIT) has been widely used in clinic, but research on its use in AN diagnosis is relatively limited. This study aims to explore the value of vHIT in the diagnosis of AN, vestibular dysfunction assessment, and postoperative compensation establishment in unilateral AN patients undergoing unilateral AN resection through labyrinthine approach.
    METHODS: This retrospective study was conducted on 27 AN patients who underwent unilateral AN resection via labyrinthine approach from October 2020 to March 2022 in the Department of Otolaryngology-Head and Neck Surgery, the Second Xiangya Hospital, Central South University. vHIT was performed 1 week before surgery to assess vestibular function, pure tone audiometry (PTA) was used to assess hearing level, and ear MRI was used to assess tumor size. Follow-up vHIT was conducted at 1 week, 1 month, 6 months, and 1 year post-surgery. The correlation of vHIT with hearing and tumor size was analyzed.
    RESULTS: Preoperative vHIT showed that the posterior semicircular canal on the affected side was the most common semicircular canal with reduced vestibulo-ocular reflex (VOR) gain. There was a correlation between the VOR gain of vHIT on the affected side and the hearing level (r=-0.47, P<0.05) or tumor size (r=-0.54, P<0.01). The results of vHIT on the affected side showed that the hearing level and mean VOR gain of the anterior semicircular canal increased slightly with time, and the amplitude and saccade percentage of the dominant saccades of the 3 semicircular canals increased, while the latency time decreased, with the most obvious changes occurring 1 week post-surgery.
    CONCLUSIONS: vHIT can effectively monitor the changes of vestibular function in AN patients before and after surgery and has application value in assisting the diagnosis of vestibular dysfunction in AN patients.
    目的: 听神经瘤(acoustic neuroma,AN)是一种良性肿瘤,通常会影响患者的听觉和前庭功能。对于AN的筛查和诊断,传统方法主要依赖于听力学检查和磁共振成像(magnetic resonance imaging,MRI),而忽略了对病变部位进行前庭功能评估的重要性。视频头脉冲试验(video head impulse test,vHIT)是一种新兴的前庭功能检测方法,已广泛应用于临床,但其应用于AN诊断的研究相对较少。本研究通过在术前及术后对经迷路入路AN切除术的单侧AN患者采用vHIT进行动态检测,以探究vHIT在AN诊断、前庭功能障碍评估、术后代偿建立中的价值。方法: 回顾性纳入2020年10月至2022年3月中南大学湘雅二医院耳鼻咽喉头颈外科的27例经迷路入路AN切除术单侧患者。术前1周进行vHIT以评估前庭功能,纯音测听(pure tone audiometry,PTA)评估听力水平,耳部MRI评估肿瘤大小;分别于术后1周、1个月、6个月、1年复查vHIT,并分析vHIT与听力、肿瘤大小之间的相关性。结果: 术前vHIT显示患侧后半规管是前庭眼反射(vestibulo-ocular reflex,VOR)增益降低最常见的半规管。术前患侧vHIT的VOR增益与听力水平(r=-0.47,P<0.05)或肿瘤大小(r=-0.54,P<0.01)存在显著相关性。术后患侧vHIT结果显示水平半规管和前半规管的平均VOR增益随时间略有上升;3个半规管显性扫视的振幅和扫视波百分比均增加,而潜伏期时间缩短,并且在术后1周变化最明显。结论: vHIT能有效监测AN患者手术前后的前庭功能变化,对辅助诊断和治疗AN患者前庭功能障碍具有临床应用价值。.
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  • 文章类型: Journal Article
    最近已开发出专用的内窥镜经管经胸方法(EETTA),用于去除迷宫(行内神经鞘瘤[ILS])或内耳道(IAC)中的小型听神经瘤。尽管符合EETTA适应症的小肿瘤也是耳蜗植入(CI)的良好候选者,使用EETTA切除神经鞘瘤后,关于CI的报道很少。在这里,我们介绍了同时接受EETTA和CI的患者的结果。
    回顾性纳入了5例(2例IAC眼底肿瘤和3例ILS),这些患者在2020年至2022年期间同时接受了EETTA和CI。他们的医学图表和测试结果进行了审查。
    经过至少12个月的随访,没有严重的手术并发症,如脑膜炎,感染,或者皮肤坏死.五名患者中有四名对听觉刺激有反应。四分之三的听觉反应患者在句子识别上得分>80%。
    同时使用EETTA和CI治疗ILS和IAC眼底肿瘤是可行的。保留耳蜗神经和moduolus对于有利的CI结果很重要。因此,听力不可用的患者的ILS和IAC眼底肿瘤应尽早手术切除,以实现CI的正确听力康复。
    4级。
    UNASSIGNED: The exclusive endoscopic transcanal transpromontorial approach (EETTA) has recently been developed for the removal of small-sized acoustic neuromas in the labyrinth (intralabyrinthine schwannoma [ILS]) or internal auditory canal (IAC). Although small tumors that meet the indications for EETTA are also good candidates for cochlear implantation (CI), there are few reports on CI after schwannoma removal using EETTA. Here we present an outcome of patients who underwent simultaneous EETTA and CI.
    UNASSIGNED: Five patients (two with IAC fundus tumors and three with ILS) who underwent simultaneous EETTA and CI between 2020 and 2022 were retrospectively enrolled. Their medical charts and test results were reviewed.
    UNASSIGNED: After at least 12 months of follow-up, there were no severe surgical complications such as meningitis, infection, or skin necrosis. Four of the five patients responded to auditory stimulation. Three out of four auditory-responsive patients scored >80% on sentence recognition.
    UNASSIGNED: Simultaneous EETTA and CI are feasible for the treatment of ILS and IAC fundus tumors. Preservation of the cochlear nerve and modiolus is important for favorable CI outcomes. Therefore, ILS and IAC fundus tumors in patients with nonserviceable hearing should be surgically removed as early as possible to enable proper hearing rehabilitation with CI.
    UNASSIGNED: Level 4.
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  • 文章类型: Journal Article
    背景:前庭神经鞘瘤(VS)是前庭耳蜗神经的良性肿瘤,通常会导致严重的神经和功能损害。患者报告的结果,包括生活质量(QoL),对于了解VS及其治疗的整体影响至关重要。这项研究旨在将前庭神经鞘瘤生活质量指数(VSQOL)转化并在文化上适应德语,以扩大其与德语人群的相关性。
    方法:我们使用了定性方法,包括翻译和认知访谈,对10名接受VS手术的患者进行了访谈。翻译过程遵循TRAPD协议,以确保语言和概念的准确性。认知访谈评估了翻译问卷的可理解性和相关性。
    结果:翻译显示出显着的翻译之间的一致性,微小的差异通过协商一致解决。认知访谈提供了宝贵的见解,从而改善了项目措辞。与会者强调了关于医生转诊的额外项目的重要性,反映了美国和德国之间医疗保健系统的差异。
    结论:德国VSQOL为VS患者的QoL评估提供了一个综合工具,整合了以患者为中心的维度。正在进行验证研究,以确定其可靠性和有效性。
    BACKGROUND: Vestibular schwannomas (VSs) are benign tumors of the vestibulocochlear nerve that often cause significant neurological and functional impairment. Patient-reported outcomes, including quality of life (QoL), are essential for understanding the overall impact of VS and its treatment. This study aimed to translate and culturally adapt the Vestibular Schwannoma Quality of Life (VSQOL) Index into German to expand its relevance to German-speaking populations.
    METHODS: We used a qualitative approach including translation and cognitive interviews with 10 patients who underwent VS surgery. The translation process followed the TRAPD protocol to ensure linguistic and conceptual accuracy. Cognitive interviews assessed the comprehensibility and relevance of the translated questionnaire.
    RESULTS: The translation showed remarkable consistency between translators, with minor discrepancies resolved by consensus. Cognitive interviews provided valuable insights that led to refinements in item wording. Participants emphasized the importance of an additional item on physician referrals, reflecting differences in health care systems between the United States and Germany.
    CONCLUSIONS: The German VSQOL provides a comprehensive tool for assessing QoL in patients with VS that integrates patient-centered dimensions. A Validation study is underway to establish its reliability and validity.
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  • 文章类型: Journal Article
    背景:侧颅底(LSB)和中耳病变通常涉及面神经(FN),他们的治疗可能需要FN牺牲。无法识别的近端残端或完整的FN伴完整的FN麻痹的病例,需要与另一个运动神经进行FN吻合,以恢复对模仿肌肉组织的神经支配。中耳和LSB手术后面瘫患者的舌下神经-面神经吻合术(HFA)和咬-面神经吻合术的结果,进行了介绍和比较。
    方法:纳入中耳或LSB手术后通过舌下神经或咬肌转移吻合术恢复面神经的完全确定性面瘫的成年患者。根据HouseBrackmann分级系统(HB)对面神经功能进行分级。3个月时的面部功能结果,6个月,12个月,比较18个月和最后一次随访(超过18个月)。
    结果:153例LSB和中耳手术后出现面神经麻痹,其中HF85例(55.5%),MF68例(44.5%)。重建手术前FN麻痹的持续时间与更好的FN结果成反比。特别是具有III级HB(p=0.003)。当麻痹发作和手术复发之间的间隔为6个月或更短时,两种技术的HB评分均显着降低(MFp=0.0401;HFp=0.0022)。接受MF的患者在手术后3个月时FN功能显着改善(p=0.0078)。在最后一次随访中,63.6%恢复到III级HB,22.7%恢复到IV级。另一方面,在HF组中获得的第一个显著结果是在手术后6个月(p<0.0001).67.8%的患者在末次随访时发生HF后出现III级HB,28.8%为Ⅳ级。与HF相比,MF组手术后6个月的FN分级显着降低(p=0.0351)。这两种技术在后来的后续评估中具有统计学上相似的结果。
    MF与最初的优异结果相关,在3个月时表现出明显的面部恢复,与HF相比,手术后6个月的功能结局明显更好。尽管在这项研究中后来的结果没有显着差异,早期结果对于限制角膜暴露风险的持续时间具有重要作用.
    BACKGROUND: Lateral skull base (LSB) and middle ear pathologies often involve the facial nerve (FN), and their treatment may require FN sacrifice. Cases with unidentifiable proximal stump or intact FN with complete FN palsy, necessitate FN anastomosis with another motor nerve in order to restore innervation to the mimicking musculature. The results of hypoglossal-to-facial nerve anastomosis (HFA) and masseteric-facial nerve anastomosis in patients with facial paralysis after middle ear and LSB surgeries, are presented and compared.
    METHODS: Adult patients with total definitive facial paralysis after middle ear or LSB surgery undergoing facial nerve reanimation through hypoglossal or masseteric transfer anastomosis were enrolled. The facial nerve function was graded according to the House Brackmann grading system (HB). The facial function results at 3 months, 6 months, 12 months, 18 months and at the last follow up (more than 18 months) are compared.
    RESULTS: 153 cases of LSB and middle ear surgery presented postoperative facial palsy and underwent facial nerve reanimation surgery with HF in 85 patients (55.5%) and MF in 68 patients (44.5%). The duration of the FN palsy before reconstructive surgery was inversely associated to better FN results, in particular with having a grade III HB (p = 0.003). Both techniques had significantly lower HB scores when an interval between palsy onset and reanimation surgery was 6 months or less (MF p = 0.0401; HF p = 0.0022). Patients who underwent a MF presented significant improvement of the FN function at 3 months from surgery (p = 0.0078). At the last follow-up, 63.6% recovered to a grade III HB and 22.7% to a grade IV. On the other hand, the first significant results obtained in the HF group were at 6 months from surgery (p < 0.0001). 67.8% of patients had a grade III HB after a HF at the last follow-up, 28.8% a grade IV. FN grading at 6 months from surgery was significantly lower in the MF group compared to the HF (p = 0.0351). The two techniques had statistically similar results at later follow-up evaluations.
    UNASSIGNED: MF was associated to initial superior results, presenting significant facial recovery at 3 months, and significantly better functional outcomes at 6 months from surgery compared to HF. Although later results were not significantly different in this study, earlier results have an important role in order to limit the duration of risk of corneal exposure.
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  • 文章类型: Journal Article
    目的:在前庭神经鞘瘤(VS)显微手术中保持面神经功能,如果肿瘤紧密粘附在变薄的面神经上,一些人主张次全切除术(STR)。这项研究的目的是确定残余体积是否与进展有关,以及在STR期间是否应追求阈值残余体积以防止复发。这项研究的第二个目的是确定最后一次随访时面神经功能是否与切除程度(EOR)相关。
    方法:回顾性收集164例VS患者的临床和影像学资料。使用Visage测量肿瘤体积,并采用标准统计学方法。使用House-Brackmann量表评估手术前和末次随访时面神经功能的变化。
    结果:61例患者(37%)接受了全切除(GTR),103例(63%)接受了STR。中位临床和影像学随访时间分别为49和48个月,分别。STR后的中值残余体积为0.5cm3。Kaplan-Meier精算生存分析显示GTR后5年无进展生存率(PFS)为96.3%,高于STR后的水平(84.5%,p=0.03)。接受STR的患者的递归分区分析显示,0.60cm3的残余体积是复发的最佳阈值。残余体积≥0.60cm3的患者5年PFS为76.0%,无论佐剂SRS,低于接受GTR(96.3%)或STR(95.6%)且残留体积<0.60cm3(p<0.01)的患者。关于Cox回归分析,残余体积≥0.60cm3(HR14.4,p=0.01)与进展独立相关,即使考虑到患者年龄,辅助放射外科,和术前肿瘤大小。在最后一次治疗后至少24个月随访的112例患者中,在中位末次随访71个月时,111例(99.1%)患者实现了肿瘤控制.末次随访时更差的面神经功能与VS的先前治疗独立相关(校正OR3.7,p=0.04),但不是残余体积队列或术前肿瘤体积。
    结论:VS切除后剩余体积>0.60cm3与肿瘤进展独立相关,甚至考虑辅助SRS。这些数据支持在VS手术过程中最大化EOR,即使GTR不能安全实现。
    OBJECTIVE: To preserve facial nerve function in vestibular schwannoma (VS) microsurgery, some have advocated subtotal resection (STR) if the tumor is densely adherent to a thinned facial nerve. The objective of this study was to determine if residual volume is associated with progression and whether there is a threshold residual volume that should be pursued during STR to prevent recurrence. A secondary objective of this study was to determine whether facial nerve function at last follow-up was associated with extent of resection (EOR).
    METHODS: Clinical and radiographic data were retrospectively collected from the records of 164 patients with VS who underwent resection. Tumor volumes were measured using Visage, and standard statistical methods were used. The House-Brackmann scale was used to assess changes in facial nerve function before surgery and at last follow-up.
    RESULTS: Sixty-one patients (37%) received gross-total resection (GTR) and 103 (63%) received STR. The median clinical and radiographic follow-ups were 49 and 48 months, respectively. The median residual volume was 0.5 cm3 after STR. Kaplan-Meier actuarial survival analysis revealed a 96.3% 5-year progression-free survival (PFS) rate after GTR, which was greater than that after STR (84.5%, p = 0.03). Recursive partitioning analysis of patients receiving STR revealed a residual volume of 0.60 cm3 as the optimal threshold for recurrence. Patients with residual volume ≥ 0.60 cm3 had a 76.0% 5-year PFS, regardless of adjuvant SRS, which was lower than that for patients undergoing GTR (96.3%) or STR (95.6%) with residual volumes < 0.60 cm3 (p < 0.01). On Cox regression analysis, residual volume ≥ 0.60 cm3 (HR 14.4, p = 0.01) was independently associated with progression, even when accounting for patient age, adjuvant radiosurgery, and preoperative tumor size. In 112 patients with at least 24 months of follow-up after their last treatment, tumor control was achieved in 111 (99.1%) patients at a median last follow-up of 71 months. Worse facial nerve function at the last follow-up was independently associated with prior treatment for VS (adjusted OR 3.7, p = 0.04), but not residual volume cohort or preoperative tumor volume.
    CONCLUSIONS: Residual volume > 0.60 cm3 after VS resection was independently associated with tumor progression, even accounting for adjuvant SRS. These data support maximizing the EOR during VS surgery, even if GTR cannot be safely achieved.
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  • 文章类型: Journal Article
    雪旺氏细胞鞘是良性的来源,缓慢扩张的肿瘤被称为听神经瘤(AN)。AN的诊断和治疗方法必须以患者为中心,考虑到独特的因素和偏好。
    这项研究的目的是研究机器学习和人工智能(AI)如何彻底改变AN管理和诊断程序。
    进行了全面的系统审查,其中包括来自公共数据库的同行评审材料。关于AN的出版物,AI,直到2023年12月的深度学习都被纳入了审查的范围。
    根据我们的分析,用于体积估计的AI模型,分割,肿瘤类型分化,与健康组织的分离已经成功开发。计算生物学的发展意味着人工智能可以有效地用于各个领域,包括生活质量评估,监测,机器人辅助手术,特征提取,影像组学,图像分析,临床决策支持系统,和治疗计划。
    为了更好的诊断和治疗,各种成像方式需要强大的发展,灵活的AI模型,可以处理异构成像数据。随后的调查应该集中于再现发现,以便标准化人工智能方法,这可以改变它们在医疗环境中的用途。
    UNASSIGNED: Schwann cell sheaths are the source of benign, slowly expanding tumours known as acoustic neuromas (AN). The diagnostic and treatment approaches for AN must be patient-centered, taking into account unique factors and preferences.
    UNASSIGNED: The purpose of this study is to investigate how machine learning and artificial intelligence (AI) can revolutionise AN management and diagnostic procedures.
    UNASSIGNED: A thorough systematic review that included peer-reviewed material from public databases was carried out. Publications on AN, AI, and deep learning up until December 2023 were included in the review\'s purview.
    UNASSIGNED: Based on our analysis, AI models for volume estimation, segmentation, tumour type differentiation, and separation from healthy tissues have been developed successfully. Developments in computational biology imply that AI can be used effectively in a variety of fields, including quality of life evaluations, monitoring, robotic-assisted surgery, feature extraction, radiomics, image analysis, clinical decision support systems, and treatment planning.
    UNASSIGNED: For better AN diagnosis and treatment, a variety of imaging modalities require the development of strong, flexible AI models that can handle heterogeneous imaging data. Subsequent investigations ought to concentrate on reproducing findings in order to standardise AI approaches, which could transform their use in medical environments.
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